(4R)-3,5,5-trimethyl-4-(3-oxobutyl)cyclohex-2-en-1-one

Details

Top
Internal ID c933ee69-bff0-463b-8dd0-23c113ee0e1b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4R)-3,5,5-trimethyl-4-(3-oxobutyl)cyclohex-2-en-1-one
SMILES (Canonical) CC1=CC(=O)CC(C1CCC(=O)C)(C)C
SMILES (Isomeric) CC1=CC(=O)CC([C@H]1CCC(=O)C)(C)C
InChI InChI=1S/C13H20O2/c1-9-7-11(15)8-13(3,4)12(9)6-5-10(2)14/h7,12H,5-6,8H2,1-4H3/t12-/m0/s1
InChI Key GSTVTHMQXVKNQF-LBPRGKRZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C13H20O2
Molecular Weight 208.30 g/mol
Exact Mass 208.146329876 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 1.40
Atomic LogP (AlogP) 2.92
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (4R)-3,5,5-trimethyl-4-(3-oxobutyl)cyclohex-2-en-1-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.7846 78.46%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7810 78.10%
OATP2B1 inhibitior - 0.8532 85.32%
OATP1B1 inhibitior + 0.9112 91.12%
OATP1B3 inhibitior + 0.8795 87.95%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8238 82.38%
P-glycoprotein inhibitior - 0.9714 97.14%
P-glycoprotein substrate - 0.8331 83.31%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8750 87.50%
CYP3A4 inhibition - 0.8440 84.40%
CYP2C9 inhibition - 0.8896 88.96%
CYP2C19 inhibition - 0.8204 82.04%
CYP2D6 inhibition - 0.9259 92.59%
CYP1A2 inhibition - 0.8420 84.20%
CYP2C8 inhibition - 0.9387 93.87%
CYP inhibitory promiscuity - 0.8448 84.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.5651 56.51%
Eye corrosion - 0.9428 94.28%
Eye irritation + 0.6494 64.94%
Skin irritation + 0.5684 56.84%
Skin corrosion - 0.9861 98.61%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6129 61.29%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6107 61.07%
skin sensitisation + 0.8823 88.23%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.5719 57.19%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.4642 46.42%
Acute Oral Toxicity (c) III 0.5831 58.31%
Estrogen receptor binding - 0.8978 89.78%
Androgen receptor binding - 0.7911 79.11%
Thyroid receptor binding - 0.8845 88.45%
Glucocorticoid receptor binding - 0.8327 83.27%
Aromatase binding - 0.9449 94.49%
PPAR gamma - 0.8927 89.27%
Honey bee toxicity - 0.9395 93.95%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9825 98.25%

Targets

Top

Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.49% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.01% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.44% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.07% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.18% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.85% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.58% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.41% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.24% 96.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.07% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.58% 89.00%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Chenopodium album
Cistus creticus
Tridax procumbens

Cross-Links

Top
PubChem 14520644
LOTUS LTS0213038
wikiData Q105017766